Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:3558269-3558551 | Common:6; Rare:104 | ||||
chr2:3575098-3575358 | Common:2; Rare:73; Clinvar:3; Clinvar (benign):5 | ||||
chr2:8679141-8679238 | Rare:38 | ||||
chr2:9423168-9423283 | Common:1; Rare:26 | ||||
chr2:9423463-9423683 | Rare:70 | ||||
chr2:9555699-9556036 | Common:2; Rare:116 | ||||
chr2:9630950-9631316 | Common:3; Rare:118 | ||||
chr2:9843296-9843501 | Common:6; Rare:56 | ||||
chr2:10689934-10690004 | Common:2; Rare:22 | ||||
chr2:11746489-11746655 | Common:1; Rare:50; Clinvar:2 | ||||
chr2:15561309-15561423 | Rare:45 | ||||
chr2:17540476-17540739 | Common:1; Rare:64 | ||||
chr2:17753738-17753858 | Common:1; Rare:46 | ||||
chr2:19901664-19901743 | Common:1; Rare:38 | ||||
chr2:19990092-19990217 | Rare:31 |